Management of patients with non-atypical and atypical endometrial hyperplasia with a levonorgestrel-releasing intrauterine system: Long.-term follow-up

被引:117
作者
Wildemeersch, D. [1 ]
Janssens, D.
Pylyser, K.
De Weverc, N.
Verbeeck, G.
Dhont, M.
Tjalma, W.
机构
[1] Incubat & innovat Ctr, Gynecol Res Unit, Ghent, Belgium
[2] Gynaecol Dienst Broederstr, Turnhout, Belgium
[3] St Augustinus Hosp, Dept Anatomopathol, Veurne, Belgium
[4] St Elizabeth Hosp, Dept Anatomopathol, Turnhout, Belgium
[5] Univ hosp Ghent, Dept Obstet & Gynecol, Ghent, Belgium
[6] Univ Antwerp, Dept Obstet & Gynecol, B-2020 Antwerp, Belgium
关键词
intrauterine system (IUS); levonorgestrel (LNG); endometrial hyperplasia; long-term study; ESTROGEN SUBSTITUTION; SAFETY; AGE;
D O I
10.1016/j.maturitas.2006.12.004
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
030301 [社会学]; 100201 [内科学];
摘要
Objectives: Levonorgestrel (LNG), delivered locally into the uterine cavity has a profound effect on the endometrium. The aim of the study was to use a LNG intrauterine system to treat non-atypical and atypical endometrial hyperplasia in women and to evaluate the long-term cure (remission) rate. Methods: Each of the 20 women in the study, of whom eight were diagnosed with atypical hyperplasia, received a LNG-IUS, releasing 20 mu g LNG/day. The study is a non-comparative study with long-term follow-up (range 14-90 months). Results: All women developed a normal endometrium, except one asymptomatic woman with atypical hyperplasia who still had focal residual non-atypical hyperplasia at 3 years follow-up in the presence of a thin (<4 mm) endometrium. Conclusion: Continuous intrauterine delivery of LNG appears to be a promising alternative to hysterectomy for the treatment of endometrial hyperplasia and could enhance the success rate when compared with other routes of progestagen administration as well as intrauterine progesterone delivery. The significant reduction of the PR expression observed during treatment with the LNG-IUS appears to be a marker for the strong antiproliferative effect of the hormone at a cellular level resulting in an inhibition of estrogen bioactivity and endometrial suppression. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:210 / 213
页数:4
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